Stat3 links activated keratinocytes and immunocytes required for development of psoriasis in a novel transgenic mouse model
By S. Sano, K. Chan, Steve Carbajal, J. Clifford, M. Peavey, K. Kiguchi, S. Itami, B. Nickoloff, J. DiGiovanni. Nature Medicine, 2005
761 citations recorded by the source corpus.
Subfields: Cancer Research, Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/d250ac8f37ee8f0c36490c85faf202e0871a3d4a
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Immunology
In Oncology
Citations in the corpus
- MicroRNAs: Novel Regulators Involved in the Pathogenesis of Psoriasis? (2007, background): “In psoriasis, there is evidence for the pathogenic relevance of several different cell types that normally occur in skin: keratinocytes [12], fibroblasts [13], monocyte-derived immunocytes [11,14], T cells [15], and mast cells [16].”
- Mechanisms of cutaneous toxicities to EGFR inhibitors (2006, background): “Indeed, mice with a constitutively active STAT3 in the basal layer have a phenotype that is similar to psoriasi”
- Skin immune sentinels in health and disease (2009, background): “Furthermore, mice with constitutive activation of the transcription factor signal transducer and activator of transcription 3 (STAT3), which is downstream of cytokine receptors such as the IL-23 receptor, in keratinocytes developed a psoriasis-like conditio”